About Sollers

Sollers is a graduate school located in New Jersey, specializing in clinical research, drug safety and pharmacovigilance training.

Our graduate certificate and masters programs cover a wide range of subjects tailored to this fast growing industry, and our graduates go on to highly successful careers in the pharmaceuticals industry and healthcare industries.

  • HOURS
  • Monday - Thursday | 10 AM - 7 PM
  • Friday | 12 PM - Midnight
  • Saturday | 12 PM - Midnight
  • Sunday | Closed
  • OPEN 24/7 - sollers.edu
    • PHONE
    • (848) 299-5900
    • Location
    • 100 Menlo Park, Suite 550
      Edison New Jersey 08837 -2488

Location

Call Us Now: 848 299-5900

Sollers Blog

Doctor Erick

Recent Posts

Role of Pharmacovigilance for Drug Safety

Posted by Doctor Erick on Sep 20, 2017 12:56:40 PM

Pharmacovigilance is a vital factor to have a cohesive drug regulation system in place, in terms of tracking and assessing adverse drug reactions (ADRs). Pharmacovigilance encompasses a crucial role in the clinical research and it is showing humongous growth. Currently, the worldwide network of pharmacovigilance centers, harmonized by Uppsala Monitoring Centre, are operating on the global level for appropriate functioning of the process of drug safety monitoring across the world, according to a media statement by sbwire.com.

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Topics: Drug Safety

Life Cycle of a Pharmacist!

Posted by Doctor Erick on Aug 23, 2017 11:22:15 AM

Pharmacists are medication experts responsible for supplying quality medicines to patients as required to achieve best outcomes. He/she is a healthcare professional practicing pharmacy. Pharmacists play an important role in pharmaceutical market and pharmaceutical industry.

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Topics: Drug Safety

RBM's Key Risk Indicators- A Study!

Posted by Doctor Erick on Aug 21, 2017 1:07:43 PM

Clinical trials are part of a long and careful research process that delves into testing which medical approaches and new pharmaceutical products work best for different groups of people affected by particular medical conditions. Since their purpose is to perform research and human beings are involved in the research as participants, the trials need to follow stringent scientific standards. They also need to be monitored so as to ensure the safety of the participants.

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Topics: Clinical Research

Quality Management Systems in Drug Safety

Posted by Doctor Erick on Aug 9, 2017 12:51:29 PM

Quality is defined as one of the areas that are relatively new to drug safety and pharmacovigilance (PV). It is no longer enough to do a good job and know you’re doing a good job, but now this must be documented and reviewed by overseers to ensure that, you really are doing a good job!  In fact, one might say that, after x years of doing drug safety, “I know how to do this!”  But if one thinks about it, it is always worthwhile having another set of eyes look at someone’s work to be sure no issues or errors have slipped in.  We certainly want someone to double check airplanes and the pilot before take-off or the functioning of nuclear reactors.  So now we have it in the drug safety spectrum. With drug safety evolving into a key priority area for the biopharmaceutical industry, the emphasis on quality and compliance has increased substantially. As regulatory oversight of company safety activities for approved pharmaceutical products becomes more holistic than simply assuring adequate and compliant procedures that meet legal obligations, the system is being transformed into one that is more proactive, robust and more clinically useful.

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Topics: Drug Safety

Opportunities for Medical Students in the US

Posted by Doctor Erick on Aug 8, 2017 11:26:53 AM

The opportunities for medical students are generally classified according to the type of qualifications as such to the respective students.  There are several programs and courses that provide students with immense scope to explore in their desired medical field. 

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Topics: General Medical

Disruptive Innovations in Clinical Trials- An Overview

Posted by Doctor Erick on Aug 4, 2017 3:15:44 PM

In fact, it is really a challenging task to identify disruptive thinkers in clinical trials for the stakes are very high in the present trend. There are some of the dedicated forums conducted around the US in a delightful manner to instil potential thoughts out of people with an in-depth understanding of existing scenario in clinical trials. Such forums will be conducted as an annual event which can be relied upon by life science industry for the latest thinking in clinical trials for 21st-century drug development.

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Topics: Clinical Research

What is SAS Enterprise Guide?

Posted by Doctor Erick on Aug 3, 2017 12:39:28 PM

SAS Enterprise Guide is a point-and-click, menu and wizard-driven tool, which provides fast-track learning for quick data analysis, generates code for productivity and speeds your ability to deploy analyses and forecasts in real time.

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Topics: Data Science

Supplier Relationship Management!

Posted by Doctor Erick on Aug 2, 2017 11:39:09 AM

It was the period when McKinsey consultant Peter Kraljic defined corporate buyers to grow more proactive in supply management that Supplier Relationship Management (or SRM) came into life in the year 1983. Since then it has been a great source for the development of various sectors such as Supplier Relationship, Drug Safety and Electronic Data Capture (EDC) Clinical Data Management (CDM).

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Topics: Drug Safety

Benefits of Data-Management Plan!

Posted by Doctor Erick on Jul 31, 2017 4:12:55 PM

Data-Management Plan (DMP) is a formal document describing how you plan to handle research project data during the research and after the research is completed. It describes what tools & techniques you will use to collect, store, manage and analyze this data. Mechanism to preserve research data and means to share it with others also form a part of DMP. Most agencies, which fund the research projects, require a DMP with every funding request.

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Topics: Clinical Research

Opportunities for a Data Clinical Manager

Posted by Doctor Erick on Jul 27, 2017 1:43:43 PM

Clinical Data Management or CDM is an important area of clinical research and studies. Healthcare organizations and hospitals employ Clinical Data Managers for their organizations.

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Topics: Clinical Research